Biology 1202B Lecture Notes - Single-Nucleotide Polymorphism, Lactose Intolerance, Dna Microarray
24 Apr 2013
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17% of us have family history of multiple sclerosis. 19% of us have a family history of alzheimer"s disease. 29% of us have family history of diabetes. 56% of us have family history of baldness. 41% of us have a family history of migraines. 67% of us have a family history of cancer. All of us can smell the asparagus odour in our urine. None of us are world class sprinters. All of us have 23 pairs of chromosomes: homologous chromosomes have giemsa banding patterns. Privately held california company: clia certified lab. Developed & offer their test as a service. Dna microarray (illumina: simultaneous analysis of 960,000 snps (single nucleotide polymorphism [c g, t c]) Wanted to be leaders in understanding human genomic variation. Literature reviews have identified these 960,000 snp analysis associated with : 120 disease risks, 48 carrier statuses, 57 traits, 21 drug responses. Written report issued to you, in 2 weeks upon receiving your sample.
